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临床试验/NCT06171906
NCT06171906尚未招募4 期

Clinical Study of MSCs for Treatment of Poor Graft Function After Allogeneic Hematopoietic Stem Cell Transplantation

ShiCang Yu2 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2024年1月1日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
68
试验地点
2
主要终点
The Hemogram recovery of patients with poor graft function after treatment

研究概览

简要总结

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is an effective approach for treating both benign and malignant blood disorders. It primarily involves high-dose chemotherapy to eliminate tumor cells within the patient's body, as well as to suppress the recipient's hematopoiesis and immune function. The transplantation replaces the recipient's original hematopoietic stem cells (HSCs) with donor-derived HSCs, thereby reconstructing the donor's hematopoietic and immune functions to achieve disease cure.

Poor graft function (PGF) following transplantation, which refers to inadequate engraftment of the transplanted hematopoietic stem cells, is one of the major factors limiting the effectiveness of allo-HSCT. Mesenchymal stromal cells (MSCs), identified within the bone marrow stroma, are a type of non-hematopoietic multipotent stem cells. Several studies, including previous research by our research team, suggest that MSCs can improve the bone marrow hematopoietic microenvironment by secreting various cytokines. This leads to the promotion of hematopoietic stem cell proliferation and differentiation, enhancement of hematopoietic function, and support for hematopoiesis as well as direct or indirect promotion of vascular regeneration in damaged tissues and organs.

Therefore, exploring the efficacy of umbilical cord-derived MSCs in treating poor graft function after allo-HSCT, observing the recovery of blood parameters in patients with poor engraftment, monitoring transplantation-related complications and immune reconstitution, and conducting preliminary investigations into the underlying mechanisms can contribute to the exploration of new clinical techniques for the treatment of PGF following allo-HSCT.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Screening patients for allogeneic hematopoietic stem cell transplantation;
  • No gender limit, age ≥18 years old and ≤60 years old;
  • KPS score >60 points, expected survival period >3 months;
  • Those without serious functional damage to important organs throughout the body;
  • The patient has no other contraindications to hematopoietic stem cell transplantation
  • Voluntary test and informed consent.

排除标准

  • Have severe heart, kidney or liver dysfunction;
  • Those combined with other malignant tumors need treatment;
  • There are clinical symptoms of brain dysfunction or severe mental illness and the inability to understand or follow the research protocol;
  • Patients who cannot be guaranteed to complete the necessary treatment plan and follow-up observation;
  • Patients with severe acute allergic reactions;
  • Clinically uncontrolled active infection;
  • Patients who are participating in other clinical trials;
  • Researchers believe that the subject is not suitable for clinical trials for other reasons.

结局指标

主要结局

The Hemogram recovery of patients with poor graft function after treatment

时间窗: 20~40 days after transplantation

White blood cells: neutrophil engraftment is defined as neutrophils exceeding 0.5×10\^9/L for 3 consecutive days; red blood cells: hemoglobin is not less than 70g/L, and is free of blood transfusion; Platelets: Complete response is defined as platelet count ≥50×10\^9/L, continuous for 7 days without platelet transfusion; Partial response (PR) is defined as platelet count (20\~50)×10\^9/L, continuous Weaning from platelet transfusion at 7 days; no response (NR) is defined as 8 weeks of use at the maximum tolerated dose, platelet count \<20×10\^9/L or not weaning from platelet transfusion

次要结局

  • survival rate(1 year after transplantation)
  • Infection rate(20~40 days after transplantation)
  • graft-versus-host disease(within the initial 30 to 60 days or further)

研究者

发起方
ShiCang Yu
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

ShiCang Yu

director of Stem cell and regenerative medicine

Southwest Hospital, China

研究点 (2)

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